Pinilla I, Lund R D, Sauvé Y
Moran Eye Center, Ophthalmology and Visual Sciences, University of Utah, 75 North Medical Drive, Salt Lake City, UT 84132, USA.
Exp Eye Res. 2005 Jan;80(1):51-9. doi: 10.1016/j.exer.2004.08.012.
The Royal College of Surgeons (RCS) rat has a primary defect in retinal pigment epithelial cells that leads to the progressive loss of photoreceptors and central visual responsiveness. While most rods are lost by 90 days of age (P90), cones degenerate more slowly, and can be detected anatomically up to 2 years of age, despite massive neuronal death and retinal remodelling. To examine how this progressive degenerative process impacts on cone function, we recorded the electroretingram to white light flashes (1.37 log cd s m(-2)) presented at frequencies ranging from 3 to 50 Hz, under light adapted conditions (29.8 cd m(-2)). Pigmented dystrophic and congenic non-dystrophic RCS rats aged from 18 to 300 days were studied. In all responsive animals at all ages, maximal amplitudes were obtained at 3 Hz. In both non-dystrophic and dystrophic rats, there was an increase from P18 to P21 in response amplitude and critical fusion frequency. After P21, these two parameters declined progressively with age in dystrophic rats. Other changes included prolongation in latency, which was first detected prior to the initiation of amplitude reduction. While phase shifts were also detected in dystrophic RCS rats, they appeared at later degenerative stages. The latest age at which responses could be elicited in dystrophic rats was at P200, with positive waves being replaced by negative deflections. The effect of increments in the intensity of background illumination was tested at P50 in both groups. This caused a diminution in flicker response amplitude and critical fusion frequencies in non-dystrophics, while in dystrophic animals, response amplitudes were reduced only at low frequencies and critical fusion frequencies were unaltered. In conclusion, although dystrophic RCS rats undergo a progressive decline in cone function with age, the flicker responsiveness at P21 is comparable to that of non-dystrophic congenic rats, suggesting normal developmental maturation of the cone system in this animal model of retinal degeneration. Flicker responses can be recorded up to P200, at which point the retina has undergone severe regressive and reactive changes in its connectivity patterns. The fact that responses at this age consist of solely negative deflections might be a reflection of the highly pathological state of the retina.
皇家外科学院(RCS)大鼠的视网膜色素上皮细胞存在原发性缺陷,导致光感受器逐渐丧失和中心视觉反应性降低。虽然大多数视杆细胞在90日龄(P90)时就已丧失,但视锥细胞退化较慢,在2岁时仍可通过解剖学方法检测到,尽管此时存在大量神经元死亡和视网膜重塑。为了研究这种进行性退化过程如何影响视锥细胞功能,我们在明适应条件(29.8 cd m(-2))下,记录了对频率范围为3至50 Hz的白光闪烁(1.37 log cd s m(-2))的视网膜电图。研究了18至300日龄的色素性营养不良和同基因非营养不良的RCS大鼠。在所有年龄段的所有有反应的动物中,最大振幅在3 Hz时获得。在非营养不良和营养不良的大鼠中,从P18到P21,反应振幅和临界融合频率均有所增加。P21之后,在营养不良的大鼠中,这两个参数随年龄逐渐下降。其他变化包括潜伏期延长,这在振幅降低开始之前就已首次检测到。虽然在营养不良的RCS大鼠中也检测到了相移,但它们出现在较晚的退化阶段。营养不良的大鼠能够引发反应的最晚年龄是P200,此时正波被负向偏转所取代。在P50时测试了两组动物背景光照强度增加的影响。这导致非营养不良动物的闪烁反应振幅和临界融合频率降低,而在营养不良的动物中,仅在低频时反应振幅降低,临界融合频率未改变。总之,尽管营养不良的RCS大鼠视锥细胞功能随年龄逐渐下降,但P21时的闪烁反应性与同基因非营养不良大鼠相当,这表明在这种视网膜变性动物模型中视锥细胞系统的发育成熟正常。闪烁反应可记录到P200,此时视网膜在其连接模式上已发生严重的退行性和反应性变化。这个年龄的反应仅由负向偏转组成这一事实可能反映了视网膜的高度病理状态。